Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease
2014-01-01 Xiao, X; Yuan, J; Qing, L; Cali, I; Mikol, J; Delisle, Mb; Uro-Coste, E; Zeng, L; Abouelsaad, M; Gazgalis, D; Martinez, Mc; Wang, Gx; Brown, P; Ironside, Jw; Gambetti, P; Kong, Q; Zou, Wq.
Impaired transmissibility of atypical prions from genetic CJDG114V
2018-01-01 Cali, I; Mikhail, F; Qin, K; Gregory, C; Solanki, A; Martinez, Mc; Zhao, L; Appleby, B; Gambetti, P; Norstrom, E; Mastrianni, Ja.
Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient
2015-01-01 Del Pilar-Morales EA, ; Cali, I; Chapas, J; Bertrán-Pasarell, J; Puoti, G; Gambetti, P; Nobo, U.
Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion
2021-01-01 Brennecke, N; Cali, I; Mok, Th; Speedy, H; Genomics England Research Consortium, ; Llp, Hosszu; Stehmann, C; Cracco, L; Puoti, G; Prior, Tw; Cohen, Ml; Collins, Sj; Mead, S; Appleby, Bs.
Amyloid fibrils from the N-terminal prion protein fragment are infectious
2016-01-01 Choi, Jk; Cali, I; Surewicz, K; Kong, Q; Gambetti, P; Surewicz, Wk.
Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study
2018-01-01 Cali, I; Cohen, Ml; Haїk, S; Parchi, P; Giaccone, G; Collins, Sj; Kofskey, D; Wang, H; Mclean, Ca; Brandel, Jp; Privat, N; Sazdovitch, V; Duyckaerts, C; Kitamoto, T; Belay, Ed; Maddox, Ra; Tagliavini, F; Pocchiari, M; Leschek, E; Appleby, Bs; Safar, Jg; Schonberger, Lb; Gambetti, P
Glycoform-selective prion formation in sporadic and familial forms of prion disease
2013-01-01 Xiao, X; Yuan, J; Haïk, S; Cali, I; Zhan, Y; Moudjou, M; B, Li; Laplanche, Jl; Laude, H; Langeveld, J; Gambetti, P; Kitamoto, T; Kong, Q; Brandel, Jp; Cobb, Ba; Petersen, Rb; Zou, Wq
Molecular biology and pathology of prion strains in sporadic human prion diseases
2011-01-01 Gambetti, P; Cali, I; Notari, S; Kong, Q; Zou, Wq; Surewicz, Wk
Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type
2017-01-01 Cracco, L; Notari, S; Cali, I; Ms, Sy; Chen, Sg; Cohen, Ml; Ghetti, B; Appleby, Bs; Zou, Wq; Caughey, B; Safar, Jg; Gambetti, P
Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics
2020-01-01 Cali, I; Puoti, G; Smucny, J; Curtiss, Pm; Cracco, L; Kitamoto, T; Occhipinti, R; Cohen, Ml; Appleby, Bs; Gambetti, P
Pathologic evidence that the T188R mutation in PRNP is associated with prion disease
2010-01-01 Tartaglia, Mc; Thai, Jn; See, T; Kuo, A; Harbaugh, R; Raudabaugh, B; Cali, I; Sattavat, M; Sanchez, H; Dearmond, Sj; Geschwind, Md
Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype
2009-01-01 Ghoshal, N; Cali, I; Perrin, Rj; Josephson, Sa; Sun, N; Gambetti, P; Morris, Jc
Transmission characteristics of variably protease-sensitive prionopathy
2014-01-01 Notari, S; Xiao, X; Espinosa, Jc; Cohen, Y; Qing, L; Aguilar-Calvo, P; Kofskey, D; Cali, I; Cracco, L; Kong, Q; Torres, Jm; Zou, W; Gambetti, P
A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques
2023-01-01 Bayazid, R; Orru', C; Aslam, R; Cohen, Y; Silva-Rohwer, A; S-K, Lee; Occhipinti, R; Kong, Q; Shetty, S; Cohen M, L Cohen; Caughey, B; L B, Schonberger; B S, Appleby; Cali, I
Variable Protease-Sensitive Prionopathy Transmission to Bank Voles
2019-01-01 Nonno, R; Notari, S; Di Bari MA, ; Cali, I; Pirisinu, L; D'Agostino, C; Cracco, L; Kofskey, D; Vanni, I; Lavrich, J; Parchi, P; Agrimi, U; Gambetti, P.
Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype
2023-01-01 Cracco, L; Puoti, G; Cornacchia, A; Glisic, K; Lee, Sk; Wang, Z; Cohen, Ml; Appleby, Bs; Cali, I
Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States
2010-01-01 Notari, S; Moleres, Fj; Hunter, Sb; Belay, Ed; Schonberger, Lb; Cali, I; Parchi, P; Shieh, Wj; Brown, P; Zaki, S; Zou, Wq; Gambetti, P.
Thermodynamic stabilization of the folded domain of prion protein inhibits prion infection in vivo
2013-01-01 Kong, Q; Mills, Jl; Kundu, B; X, Li; Qing, L; Surewicz, K; Cali, I; Huang, S; Zheng, M; Swietnicki, W; Sönnichsen, Fd; Gambetti, P; Surewicz, Wk
Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone
2015-01-01 Cali, I; Miller, Cj; Parisi, Je; Geschwind, Md; Gambetti, P; Schonberger, Lb
Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases
2013-01-01 Kim, Mo; Cali, I; Oehler, A; Fong, Jc; Wong, K; See, T; Katz, Js; Gambetti, P; Bettcher, Bm; Dearmond, Sj; Geschwind, Md
| Titolo | Data di pubblicazione | Autore(i) | File |
|---|---|---|---|
| Comparative Study of Prions in Iatrogenic and Sporadic Creutzfeldt-Jakob Disease | 1-gen-2014 | Xiao, X; Yuan, J; Qing, L; Cali, I; Mikol, J; Delisle, Mb; Uro-Coste, E; Zeng, L; Abouelsaad, M; Gazgalis, D; Martinez, Mc; Wang, Gx; Brown, P; Ironside, Jw; Gambetti, P; Kong, Q; Zou, Wq. | |
| Impaired transmissibility of atypical prions from genetic CJDG114V | 1-gen-2018 | Cali, I; Mikhail, F; Qin, K; Gregory, C; Solanki, A; Martinez, Mc; Zhao, L; Appleby, B; Gambetti, P; Norstrom, E; Mastrianni, Ja. | |
| Sporadic Creutzfeldt-Jakob disease in a native Puerto Rican patient | 1-gen-2015 | Del Pilar-Morales EA, ; Cali, I; Chapas, J; Bertrán-Pasarell, J; Puoti, G; Gambetti, P; Nobo, U. | |
| Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion | 1-gen-2021 | Brennecke, N; Cali, I; Mok, Th; Speedy, H; Genomics England Research Consortium, ; Llp, Hosszu; Stehmann, C; Cracco, L; Puoti, G; Prior, Tw; Cohen, Ml; Collins, Sj; Mead, S; Appleby, Bs. | |
| Amyloid fibrils from the N-terminal prion protein fragment are infectious | 1-gen-2016 | Choi, Jk; Cali, I; Surewicz, K; Kong, Q; Gambetti, P; Surewicz, Wk. | |
| Iatrogenic Creutzfeldt-Jakob disease with Amyloid-β pathology: an international study | 1-gen-2018 | Cali, I; Cohen, Ml; Haїk, S; Parchi, P; Giaccone, G; Collins, Sj; Kofskey, D; Wang, H; Mclean, Ca; Brandel, Jp; Privat, N; Sazdovitch, V; Duyckaerts, C; Kitamoto, T; Belay, Ed; Maddox, Ra; Tagliavini, F; Pocchiari, M; Leschek, E; Appleby, Bs; Safar, Jg; Schonberger, Lb; Gambetti, P | |
| Glycoform-selective prion formation in sporadic and familial forms of prion disease | 1-gen-2013 | Xiao, X; Yuan, J; Haïk, S; Cali, I; Zhan, Y; Moudjou, M; B, Li; Laplanche, Jl; Laude, H; Langeveld, J; Gambetti, P; Kitamoto, T; Kong, Q; Brandel, Jp; Cobb, Ba; Petersen, Rb; Zou, Wq | |
| Molecular biology and pathology of prion strains in sporadic human prion diseases | 1-gen-2011 | Gambetti, P; Cali, I; Notari, S; Kong, Q; Zou, Wq; Surewicz, Wk | |
| Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type | 1-gen-2017 | Cracco, L; Notari, S; Cali, I; Ms, Sy; Chen, Sg; Cohen, Ml; Ghetti, B; Appleby, Bs; Zou, Wq; Caughey, B; Safar, Jg; Gambetti, P | |
| Co-existence of PrPD types 1 and 2 in sporadic Creutzfeldt-Jakob disease of the VV subgroup: phenotypic and prion protein characteristics | 1-gen-2020 | Cali, I; Puoti, G; Smucny, J; Curtiss, Pm; Cracco, L; Kitamoto, T; Occhipinti, R; Cohen, Ml; Appleby, Bs; Gambetti, P | |
| Pathologic evidence that the T188R mutation in PRNP is associated with prion disease | 1-gen-2010 | Tartaglia, Mc; Thai, Jn; See, T; Kuo, A; Harbaugh, R; Raudabaugh, B; Cali, I; Sattavat, M; Sanchez, H; Dearmond, Sj; Geschwind, Md | |
| Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype | 1-gen-2009 | Ghoshal, N; Cali, I; Perrin, Rj; Josephson, Sa; Sun, N; Gambetti, P; Morris, Jc | |
| Transmission characteristics of variably protease-sensitive prionopathy | 1-gen-2014 | Notari, S; Xiao, X; Espinosa, Jc; Cohen, Y; Qing, L; Aguilar-Calvo, P; Kofskey, D; Cali, I; Cracco, L; Kong, Q; Torres, Jm; Zou, W; Gambetti, P | |
| A novel subtype of sporadic Creutzfeldt-Jakob disease with PRNP codon 129MM genotype and PrP plaques | 1-gen-2023 | Bayazid, R; Orru', C; Aslam, R; Cohen, Y; Silva-Rohwer, A; S-K, Lee; Occhipinti, R; Kong, Q; Shetty, S; Cohen M, L Cohen; Caughey, B; L B, Schonberger; B S, Appleby; Cali, I | |
| Variable Protease-Sensitive Prionopathy Transmission to Bank Voles | 1-gen-2019 | Nonno, R; Notari, S; Di Bari MA, ; Cali, I; Pirisinu, L; D'Agostino, C; Cracco, L; Kofskey, D; Vanni, I; Lavrich, J; Parchi, P; Agrimi, U; Gambetti, P. | |
| Novel histotypes of sporadic Creutzfeldt-Jakob disease linked to 129MV genotype | 1-gen-2023 | Cracco, L; Puoti, G; Cornacchia, A; Glisic, K; Lee, Sk; Wang, Z; Cohen, Ml; Appleby, Bs; Cali, I | |
| Multiorgan detection and characterization of protease-resistant prion protein in a case of variant CJD examined in the United States | 1-gen-2010 | Notari, S; Moleres, Fj; Hunter, Sb; Belay, Ed; Schonberger, Lb; Cali, I; Parchi, P; Shieh, Wj; Brown, P; Zaki, S; Zou, Wq; Gambetti, P. | |
| Thermodynamic stabilization of the folded domain of prion protein inhibits prion infection in vivo | 1-gen-2013 | Kong, Q; Mills, Jl; Kundu, B; X, Li; Qing, L; Surewicz, K; Cali, I; Huang, S; Zheng, M; Swietnicki, W; Sönnichsen, Fd; Gambetti, P; Surewicz, Wk | |
| Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone | 1-gen-2015 | Cali, I; Miller, Cj; Parisi, Je; Geschwind, Md; Gambetti, P; Schonberger, Lb | |
| Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases | 1-gen-2013 | Kim, Mo; Cali, I; Oehler, A; Fong, Jc; Wong, K; See, T; Katz, Js; Gambetti, P; Bettcher, Bm; Dearmond, Sj; Geschwind, Md |
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